Variant #0000519902 (NC_000003.11:g.46009685dup, NM_024513.3:c.1141dup (FYCO1))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.46009685dup
DNA change (hg38) g.45968193dup
Published as FYCO1(NM_024513.3):c.1141dupA (p.T381Nfs*15)
ISCN -
DB-ID CXCR6_000013
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-12 18:48:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXCR6 NM_006564.1 +/. - c.*20683dup r.(?) p.(=)
FYCO1 NM_024513.3 +/. - c.1141dup r.(?) p.(Thr381AsnfsTer15)


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